Package 51662-1388-1

Brand: hydralazine hydrochloride

Generic: hydralazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1388-1
Digits Only 5166213881
Product NDC 51662-1388
Product ID 51662-1388_2b377557-c2e1-ba26-e063-6394a90a64ad
Description

1 mL in 1 VIAL, SINGLE-DOSE (51662-1388-1)

Marketing

Marketing Status
Marketed Since 2019-10-07
Brand hydralazine hydrochloride
Generic hydralazine hydrochloride
Sample Package No

Linked Drug Pages (1)

HYDRALAZINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "2b377557-c2e1-ba26-e063-6394a90a64ad", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["966571"], "spl_set_id": ["94530e4d-b1c0-6171-e053-2a95a90a05fa"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (51662-1388-1)", "package_ndc": "51662-1388-1", "marketing_start_date": "20191007"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "51662-1388_2b377557-c2e1-ba26-e063-6394a90a64ad", "dosage_form": "INJECTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "51662-1388", "generic_name": "HYDRALAZINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDRALAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA040730", "marketing_category": "ANDA", "marketing_start_date": "20191007", "listing_expiration_date": "20261231"}